TRAPPC6A
Trafficking protein particle complex subunit 6A
Also known as: HSPC289, MGC2650, TPC6A_HUMAN, TRS33
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75865
- Gene
- TRAPPC6A
- Ensembl
- ENSG00000007255
- Chromosome
- 19
- Canonical length
- 159 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a component of the trafficking protein particle complex, which tethers transport vesicles to the cis-Golgi membrane. Loss of expression of the related gene in mouse affects coat and eye pigmentation, suggesting that the encoded protein may be involved in melanosome biogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]
Canonical amino-acid sequenceUniProt
159 residues, UniProt reviewed canonical sequence.
>O75865|TRAPPC6A
1 MADTVLFEFL HTEMVAELWA HDPDPGPGGQ KMSLSVLEGM GFRVGQALGE RLPRETLAFR
61 EELDVLKFLC KDLWVAVFQK QMDSLRTNHQ GTYVLQDNSF PLLLPMASGL QYLEEAPKFL
121 AFTCGLLRGA LYTLGIESVV TASVAALPVC KFQVVIPKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRAPPC6A can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 63 nTPM
Expression across tissuesHPA
Tissue
- kidney: 63 nTPM
- liver: 58 nTPM
- skin: 53 nTPM
- spinal cord: 48 nTPM
- bone marrow: 46 nTPM
- spleen: 41 nTPM
Single-cell type
- late spermatids: 164 nCPM
- epididymal principal cells: 159 nCPM
- cytotrophoblasts: 147 nCPM
- epididymal efferent duct absorptive cells: 141 nCPM
- migrating cytotrophoblasts: 110 nCPM
- fallopian secretory cells: 101 nCPM
Immune cell
- NK-cell: 114 nTPM
- T-reg: 113 nTPM
- naive CD4 T-cell: 111 nTPM
- memory CD4 T-cell: 106 nTPM
- naive CD8 T-cell: 95 nTPM
- MAIT T-cell: 95 nTPM
Brain region
- white matter: 39 nTPM
- medulla oblongata: 35 nTPM
- basal ganglia: 32 nTPM
- cerebellum: 30 nTPM
- pons: 29 nTPM
- spinal cord: 29 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.87
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.02
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TRAPPC6A in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TRAPPC6A as an antibody target. Whether an autoantibody or antibody against TRAPPC6A could matter depends on whether native TRAPPC6A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRAPPC6A is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TRAPPC6A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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